106401-57-4 Usage
Uses
Used in Pharmaceutical Industry:
2-O-Benzyl-3-O-allyl-sn-glycerol is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure allows for the creation of novel molecules with potential therapeutic properties.
Used in Lipid Chemistry:
In the field of lipid chemistry, 2-O-Benzyl-3-O-allyl-sn-glycerol is used as a precursor for the synthesis of phospholipids or ether lipids. These lipids are essential components of cell membranes and have various biological functions, making them important targets for research and drug development.
Used in Cosmetics Industry:
2-O-Benzyl-3-O-allyl-sn-glycerol may also find applications in the cosmetics industry, where it can be used as a component in the formulation of skincare and hair care products. Its unique structure could potentially contribute to the development of innovative products with enhanced properties.
Used in Research and Development:
As a synthetic intermediate, 2-O-Benzyl-3-O-allyl-sn-glycerol is valuable in research and development for the creation of new compounds with potential applications in various fields, including pharmaceuticals, materials science, and biotechnology. Its versatility makes it a useful tool for scientists and researchers working on the development of novel molecules and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 106401-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106401-57:
(8*1)+(7*0)+(6*6)+(5*4)+(4*0)+(3*1)+(2*5)+(1*7)=84
84 % 10 = 4
So 106401-57-4 is a valid CAS Registry Number.
106401-57-4Relevant academic research and scientific papers
Synthesis of novel mimetics of the sialyl Lewis X determinant
Toepfer,Toepfer, Alexander,Kretzschmar,Kretzschmar, Gerhard,Bartnik,Bartnik, Eckart
, p. 9161 - 9164 (2007/10/02)
Mimetics of the sialyl Lewis-X determinant in which at least one sugar domain is simulated by a di-, tri- or tetraalcohol unit have been synthesized. The inhibitory potency of these compounds for E- and P-selectin mediated cell adhesion has been evaluated in cell culture assays. The receptor binding affinity of the best of these mimetics was slightly higher than that of the natural oligosaccharide ligand sialyl Lewis X.
The Chemistry of L-Ascorbic and D-Isoascorbic Acids. 2. R and S Glyceraldehydes from a Common Intermediate
Mikkilineni, Amarendra B.,Kumar, Praveen,Abushanab, Elie
, p. 6005 - 6009 (2007/10/02)
(R)- and (S)-glyceraldehyde and glycerol derivatives have been prepared from (2R,3S)-1,2-O-isopropylidenebutane-1,2,3,4-tetrol. (2R,3S)- and (2S,3S)-1,2-O-benzylidenebutane-1,2,3,4-tetrol have been prepared and cleaved to give (R)- and (S)-1,2-O-benzylideneglyceraldehydes and -glycerols.The conservation of chirality and conversion to PAF analogues are also demonstrated.
SYNTHESIS OF A LIPOTEICHOIC ACID-CARRIER FRAGMENT OF Staphylococcus aureus
Oltvoort, Jan J.,Kloosterman, Marcel,Boeckel, Constant A. A. van,Boom, Jacques H. van
, p. 147 - 164 (2007/10/02)
A lipoteichoic acid-carrier fragment containing three glycerol units and one glycolipid unit was synthesized by use of the bifunctional phosphorylating reagents bis(1-benzotriazolyl) 2,2,2-tribromoethyl and 2-chlorophenyl phosphates.Protection of the sn-g
